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在加速药物研发合作组织中,伴有低蛋白尿的 SLE 患者中增殖性和膜性肾炎的发病率较高。

High incidence of proliferative and membranous nephritis in SLE patients with low proteinuria in the Accelerating Medicines Partnership.

机构信息

Department of Medicine, New York University School of Medicine, New York, NY.

Division of Rheumatology, Department of Medicine, Johns Hopkins University, Baltimore, MD.

出版信息

Rheumatology (Oxford). 2022 Nov 2;61(11):4335-4343. doi: 10.1093/rheumatology/keac067.

DOI:10.1093/rheumatology/keac067
PMID:35212719
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9629353/
Abstract

OBJECTIVE

Delayed detection of LN associates with worse outcomes. There are conflicting recommendations regarding a threshold level of proteinuria at which biopsy will likely yield actionable management. This study addressed the association of urine protein:creatinine ratios (UPCR) with clinical characteristics and investigated the incidence of proliferative and membranous histology in patients with a UPCR between 0.5 and 1.

METHODS

A total of 275 SLE patients (113 first biopsy, 162 repeat) were enrolled in the multicentre multi-ethnic/racial Accelerating Medicines Partnership across 15 US sites at the time of a clinically indicated renal biopsy. Patients were followed for 1 year.

RESULTS

At biopsy, 54 patients had UPCR <1 and 221 had UPCR ≥1. Independent of UPCR or biopsy number, a majority (92%) of patients had class III, IV, V or mixed histology. Moreover, patients with UPCR <1 and class III, IV, V, or mixed had a median activity index of 4.5 and chronicity index of 3, yet 39% of these patients had an inactive sediment. Neither anti-dsDNA nor low complement distinguished class I or II from III, IV, V or mixed in patients with UPCR <1. Of 29 patients with baseline UPCR <1 and class III, IV, V or mixed, 23 (79%) had a UPCR <0.5 at 1 year.

CONCLUSION

In this prospective study, three-quarters of patients with UPCR <1 had histology showing class III, IV, V or mixed with accompanying activity and chronicity despite an inactive sediment or normal serologies. These data support renal biopsy at thresholds lower than a UPCR of 1.

摘要

目的

LN 的延迟检测与更差的结果相关。对于蛋白尿水平达到何种程度进行活检可能会获得可操作的管理,目前存在相互矛盾的建议。本研究旨在探讨尿蛋白与肌酐比值(UPCR)与临床特征的关系,并调查 UPCR 在 0.5 至 1 之间的患者中增生性和膜性组织学的发生率。

方法

在临床指示性肾活检时,共招募了 275 名 SLE 患者(113 名首次活检,162 名重复),这些患者来自美国 15 个地点的加速药物合作联盟的多中心多民族/种族研究。患者随访 1 年。

结果

在活检时,54 名患者的 UPCR <1,221 名患者的 UPCR ≥1。独立于 UPCR 或活检数量,大多数(92%)患者的组织学为 III、IV、V 或混合性。此外,UPCR <1 且具有 III、IV、V 或混合性的患者的活动指数中位数为 4.5,慢性指数为 3,但 39%的这些患者的尿液沉渣处于不活动状态。在 UPCR <1 的患者中,既没有抗 dsDNA 也没有低补体可以区分 I 类或 II 类与 III、IV、V 或混合性。在基线 UPCR <1 且具有 III、IV、V 或混合性的 29 名患者中,23 名(79%)在 1 年内 UPCR <0.5。

结论

在这项前瞻性研究中,尽管尿液沉渣处于不活动状态或血清学正常,但四分之三的 UPCR <1 的患者的组织学显示出 III、IV、V 或混合性,伴有活动和慢性。这些数据支持在 UPCR 低于 1 的阈值下进行肾活检。

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Efficacy and safety of voclosporin versus placebo for lupus nephritis (AURORA 1): a double-blind, randomised, multicentre, placebo-controlled, phase 3 trial.与安慰剂相比,voclosporin治疗狼疮性肾炎的疗效和安全性(AURORA 1):一项双盲、随机、多中心、安慰剂对照的3期试验。
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